Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865383Generated: October 26, 2026

Cyclohexane → 2-Bromo-3-isopropoxy-propenal

https://huagongshe.com/reaction/865383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
Reactant2-BromopropanedialHCID 74945—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventIsopropanolHCID 3776—
Product2-Bromo-3-isopropoxy-propenalHCID 53416634103%

Reaction Steps

With moderate agitation, a 20 gallon reactor system was charged with cyclohexane (29.12 L), 2-bromo-malonaldehyde (2.33 kg), p-toluenesulfonic acid monohydrate 43.94 g, and 2-propanol (4.65 L). The contents of the reactor were heated to allow for the removal of distillate under atmospheric pressure (jacket temp. 95° C. and process temp. at 66.4° C.). A total of 16 L of distillate was removed from the reaction via the cooling tower. This represents approximately 47% of the total volume of cyclohexane/2-propanol (33.77 L) being removed from the reactor. The reaction solution was cooled to near ambient temperature and transferred to a 10 gallon reactor system at 40° C. An additional 6 L of distillate was removed under vacuum (~64 torr, jacket temp. 62° C., and reaction temp. 25° C.). The mobile dark orange oil was drained from the vessel and transferred to a rotary evaporator receiver flask and further concentrated under house vacuum at ~30° C. using a rotary evaporator. About 0.2 L more of solvent was removed. Total product obtained was 3.072 kg (16 mol, 103% yield). The product was used as obtained in the next step. This material is unstable and must be kept in a freezer (<-5° C., under nitrogen). The shelve-life is about 2 weeks.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565577
Source datasetuspto-grants-1996_10
ORD IDord-17dc28bbfe19407aba92a68e81530d6e
Source noteuspto-grants-1996_10